UA81902C2 - Кремнийорганичнеские соединения, способ их получения, каучуковые смеси, которые содержат их, и применение каучуковых смесей - Google Patents
Кремнийорганичнеские соединения, способ их получения, каучуковые смеси, которые содержат их, и применение каучуковых смесей Download PDFInfo
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- UA81902C2 UA81902C2 UA20040604824A UA20040604824A UA81902C2 UA 81902 C2 UA81902 C2 UA 81902C2 UA 20040604824 A UA20040604824 A UA 20040604824A UA 20040604824 A UA20040604824 A UA 20040604824A UA 81902 C2 UA81902 C2 UA 81902C2
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- rubber
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- ethanol
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- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 108700013882 rat DE Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- YWWOEPOBDHZQEJ-UHFFFAOYSA-N s-(4-cyclohexyl-1,3-benzothiazol-2-yl)thiohydroxylamine Chemical compound C1=CC=C2SC(SN)=NC2=C1C1CCCCC1 YWWOEPOBDHZQEJ-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical class OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 1
- XSIGLRIVXRKQRA-UHFFFAOYSA-N triethoxysilylmethanethiol Chemical compound CCO[Si](CS)(OCC)OCC XSIGLRIVXRKQRA-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 235000014101 wine Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/548—Silicon-containing compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
В заявке описываются кремнийорганические соединения общей формулы І , І которые получают катализированным взаимодействием силанов общей формулы ІІ , ІІ со спиртами общей формулы R'-OH при отщеплении RIV-ОН-группы, при этом молярное соотношение между R'-OH и RIV-О-группами составляет, по меньшей мере 1, и RIV-OH-группу в непрерывном или периодическом режиме отделяют от реакционной смеси. Предложенные в изобретении кремнийорганические смеси могут применяться как промоторы адгезии в каучуковых смесях с укрепляющими наполнителями.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10327624A DE10327624B3 (de) | 2003-06-20 | 2003-06-20 | Organosiliciumverbindungen, Verfahren zu ihrer Herstellung, sowie ihre Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA81902C2 true UA81902C2 (ru) | 2008-02-25 |
Family
ID=33394880
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA20040604824A UA81902C2 (ru) | 2003-06-20 | 2004-06-18 | Кремнийорганичнеские соединения, способ их получения, каучуковые смеси, которые содержат их, и применение каучуковых смесей |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7423165B2 (ru) |
| EP (1) | EP1491547B1 (ru) |
| JP (1) | JP4606785B2 (ru) |
| KR (1) | KR101122952B1 (ru) |
| CN (1) | CN100390182C (ru) |
| AT (1) | ATE312108T1 (ru) |
| BR (1) | BRPI0402414B1 (ru) |
| DE (2) | DE10327624B3 (ru) |
| ES (1) | ES2250943T3 (ru) |
| IL (1) | IL162623A0 (ru) |
| MX (1) | MXPA04006052A (ru) |
| MY (1) | MY134485A (ru) |
| PL (1) | PL1491547T3 (ru) |
| RU (1) | RU2348642C2 (ru) |
| TW (1) | TWI353999B (ru) |
| UA (1) | UA81902C2 (ru) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10362060B4 (de) * | 2003-10-21 | 2009-07-09 | Altana Coatings & Sealants Gmbh | Verpackungsmaterial mit einer Barriereschicht für Gase |
| DE102004049427A1 (de) | 2004-10-08 | 2006-04-13 | Degussa Ag | Polyetherfunktionelle Siloxane, polyethersiloxanhaltige Zusammensetzungen, Verfahren zu deren Herstellung und deren Verwendung |
| DE102005057801A1 (de) | 2005-01-20 | 2006-08-03 | Degussa Ag | Mercaptosilane |
| DE102005004872A1 (de) * | 2005-02-03 | 2006-08-10 | Degussa Ag | Wässrige Emulsionen von funktionellen Alkoxysilanen und deren kondensierten Oligomeren, deren Herstellung und Verwendung zur Oberflächenbehandlung |
| CN101180344B (zh) * | 2005-03-24 | 2012-01-11 | 株式会社普利司通 | 具有低挥发性有机化合物（voc）释放的配混二氧化硅补强橡胶 |
| DE102005020535B3 (de) * | 2005-05-03 | 2006-06-08 | Degussa Ag | Verfahren zur Herstellung von Mercaptoorganyl(alkoxysilanen) |
| DE102005038791A1 (de) * | 2005-08-17 | 2007-02-22 | Degussa Ag | Organosiliciumverbindungen, ihre Herstellung und ihre Verwendung |
| DE102005051921A1 (de) * | 2005-10-29 | 2007-05-03 | Henkel Kgaa | α-Ethoxysilan modifizierte Polymere, deren Herstellung und Verwendung |
| DE102005060122A1 (de) * | 2005-12-16 | 2007-06-21 | Degussa Gmbh | Verfahren zur Herstellung von (Mercaptoorganyl)alkylpolyethersilanen |
| DE102006004062A1 (de) * | 2006-01-28 | 2007-08-09 | Degussa Gmbh | Kautschukmischungen |
| US7919650B2 (en) * | 2006-02-21 | 2011-04-05 | Momentive Performance Materials Inc. | Organofunctional silanes and their mixtures |
| DE102006013090A1 (de) * | 2006-03-20 | 2007-09-27 | Georg-August-Universität Göttingen | Kompositwerkstoff aus Holz und thermoplastischem Kunststoff |
| DE102006027235A1 (de) * | 2006-06-09 | 2008-01-17 | Evonik Degussa Gmbh | Kautschukmischungen |
| US7550524B2 (en) * | 2006-10-06 | 2009-06-23 | Momentive Performance Materials Inc. | Elastomer composition containing mercaptofunctional silane and process for making same |
| PL1982964T3 (pl) | 2007-04-20 | 2019-08-30 | Evonik Degussa Gmbh | Mieszanina zawierająca związek krzemoorganiczny i jej zastosowanie |
| US8501895B2 (en) | 2007-05-23 | 2013-08-06 | Bridgestone Corporation | Method for making alkoxy-modified silsesquioxanes and amino alkoxy-modified silsesquioxanes |
| US7915368B2 (en) | 2007-05-23 | 2011-03-29 | Bridgestone Corporation | Method for making alkoxy-modified silsesquioxanes |
| DE102007037556A1 (de) | 2007-08-09 | 2009-02-12 | Evonik Degussa Gmbh | Verfahren zur Herstellung von alkylpolyethersubstituierten Mercaptosilanen |
| DE102007038313A1 (de) * | 2007-08-14 | 2009-02-19 | Evonik Degussa Gmbh | Anorganisch-modifizierte Polyesterbindemittelzubereitung, Verfahren zur Herstellung und ihre Verwendung |
| DE102007038314A1 (de) | 2007-08-14 | 2009-04-16 | Evonik Degussa Gmbh | Verfahren zur kontrollierten Hydrolyse und Kondensation von Epoxy-funktionellen Organosilanen sowie deren Condensation mit weiteren organofunktionellen Alkoxysilanen |
| DE102007040246A1 (de) | 2007-08-25 | 2009-02-26 | Evonik Degussa Gmbh | Strahlenhärtbare Formulierungen |
| DE102007045186A1 (de) * | 2007-09-21 | 2009-04-09 | Continental Teves Ag & Co. Ohg | Rückstandsfreies, schichtbildendes, wässriges Versiegelungssystem für metallische Oberflächen auf Silan-Basis |
| US8962746B2 (en) | 2007-12-27 | 2015-02-24 | Bridgestone Corporation | Methods of making blocked-mercapto alkoxy-modified silsesquioxane compounds |
| US8097674B2 (en) | 2007-12-31 | 2012-01-17 | Bridgestone Corporation | Amino alkoxy-modified silsesquioxanes in silica-filled rubber with low volatile organic chemical evolution |
| US8794282B2 (en) | 2007-12-31 | 2014-08-05 | Bridgestone Corporation | Amino alkoxy-modified silsesquioxane adhesives for improved metal adhesion and metal adhesion retention to cured rubber |
| DE102008001808A1 (de) * | 2008-05-15 | 2009-11-19 | Evonik Degussa Gmbh | Beschichtungszusammensetzung |
| EP2119737B1 (en) * | 2008-05-15 | 2011-05-04 | Evonik Degussa GmbH | Electronic packaging |
| DE102008001855A1 (de) * | 2008-05-19 | 2009-11-26 | Evonik Degussa Gmbh | Zweikomponenten-Zusammensetzung zur Herstellung von flexiblen Polyurethan-Gelcoats |
| DE102008041918A1 (de) * | 2008-09-09 | 2010-03-11 | Evonik Degussa Gmbh | Silanolkondensationskatalysatoren zur Vernetzung von gefüllten und ungefüllten Polymer-Compounds |
| DE102008041919A1 (de) * | 2008-09-09 | 2010-03-11 | Evonik Degussa Gmbh | Verwendung von Silicium enthaltenden Vorläuferverbindungen einer organischen Säure als Katalysator zur Vernetzung von gefüllten und ungefüllten Polymer-Compounds |
| JP5503137B2 (ja) * | 2008-12-04 | 2014-05-28 | 株式会社ブリヂストン | 有機ケイ素化合物、並びにそれを用いたゴム組成物及びタイヤ |
| FR2945815B1 (fr) * | 2009-05-20 | 2011-07-01 | Michelin Soc Tech | Composition de caoutchouc comportant un agent de couplage organosilane |
| US8642691B2 (en) | 2009-12-28 | 2014-02-04 | Bridgestone Corporation | Amino alkoxy-modified silsesquioxane adhesives for improved metal adhesion and metal adhesion retention to cured rubber |
| JP5831354B2 (ja) | 2011-05-16 | 2015-12-09 | 信越化学工業株式会社 | ゴム用配合剤、ゴム組成物及びタイヤ |
| JP2012240924A (ja) | 2011-05-16 | 2012-12-10 | Shin-Etsu Chemical Co Ltd | 有機ケイ素化合物及びその製造方法、ゴム用配合剤、ゴム組成物並びにタイヤ |
| JP2013119529A (ja) | 2011-12-07 | 2013-06-17 | Shin-Etsu Chemical Co Ltd | 有機ケイ素化合物及びその製造方法、ゴム用配合剤並びにゴム組成物 |
| MX356323B (es) * | 2012-09-14 | 2018-05-23 | Trinseo Europe Gmbh | Polimeros elastomericos modificados por sulfuro de silano. |
| JP6026902B2 (ja) * | 2013-01-30 | 2016-11-16 | 住友ゴム工業株式会社 | タイヤ用ゴム組成物及び空気入りタイヤ |
| JP6248597B2 (ja) | 2013-12-13 | 2017-12-20 | 信越化学工業株式会社 | 含硫黄有機ケイ素化合物及びその製造方法、ゴム用配合剤、並びにゴム組成物 |
| US10428203B2 (en) | 2014-09-08 | 2019-10-01 | Sumitomo Rubber Industries, Ltd. | Pneumatic tire |
| EP3241221A4 (en) | 2014-12-31 | 2018-08-08 | Bridgestone Corporation | Amino alkoxy-modified silsesquioxane adhesives for adhering steel alloy to rubber |
| JP6384338B2 (ja) | 2015-01-26 | 2018-09-05 | 信越化学工業株式会社 | オルガノポリシロキサン、ゴム用配合剤、ゴム組成物及びタイヤ |
| JP6866348B2 (ja) * | 2015-07-29 | 2021-04-28 | 株式会社ブリヂストン | 官能化されたポリマーの調製方法、関連の官能化化合物、及びその調製 |
| JP6716942B2 (ja) | 2016-02-18 | 2020-07-01 | 住友ゴム工業株式会社 | 空気入りタイヤ及び空気入りタイヤの製造方法 |
| JP6128247B2 (ja) | 2016-03-10 | 2017-05-17 | 信越化学工業株式会社 | 有機ケイ素化合物、並びにそれを用いたゴム用配合剤およびゴム組成物 |
| JP6183497B2 (ja) | 2016-05-23 | 2017-08-23 | 信越化学工業株式会社 | ゴム組成物 |
| JP6638603B2 (ja) | 2016-09-07 | 2020-01-29 | 信越化学工業株式会社 | ゴム用配合剤およびゴム組成物 |
| JP6972534B2 (ja) | 2016-10-31 | 2021-11-24 | 住友ゴム工業株式会社 | 混練機投入用ポリマー |
| JP6862787B2 (ja) | 2016-11-22 | 2021-04-21 | 住友ゴム工業株式会社 | 空気入りタイヤ |
| DE102017221282A1 (de) * | 2017-11-28 | 2019-05-29 | Evonik Degussa Gmbh | Silanmischungen und Verfahren zu deren Herstellung |
| DE102017221259A1 (de) | 2017-11-28 | 2019-05-29 | Evonik Degussa Gmbh | Silanmischungen und Verfahren zu deren Herstellung |
| CN109762014B (zh) * | 2019-03-05 | 2021-03-26 | 湖北江瀚新材料股份有限公司 | 一种固体含硫硅烷的制备方法 |
| KR102256972B1 (ko) * | 2019-05-21 | 2021-05-27 | 이갑진 | 신발 밑창용 조성물 |
| JP2021046357A (ja) * | 2019-09-17 | 2021-03-25 | 信越化学工業株式会社 | 有機ケイ素化合物、有機ケイ素化合物の混合物およびその製造方法、有機ケイ素化合物の混合物を含有するゴム組成物並びにタイヤ |
| JP2021130730A (ja) | 2020-02-18 | 2021-09-09 | 信越化学工業株式会社 | オルガノポリシロキサン、ゴム組成物およびタイヤ |
| JP7484212B2 (ja) * | 2020-02-21 | 2024-05-16 | 住友ゴム工業株式会社 | タイヤ |
| CN113337010B (zh) * | 2020-03-02 | 2022-05-20 | 北京化工大学 | 一种炭黑用偶联剂及其制备方法和应用 |
| EP4145118A1 (en) * | 2021-09-02 | 2023-03-08 | Sumitomo Rubber Industries, Ltd. | Method for evaluation of chemical bond presence or absence by multidimensional nmr |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1520022C3 (de) * | 1964-12-09 | 1973-10-31 | Th. Goldschmidt Ag, 4300 Essen | Verfahren zur Herstellung von schwefelhaltigen, mit organischen SiIi ciumverbindungen modifizierten Epoxid harzen |
| JPS62181346A (ja) | 1986-02-05 | 1987-08-08 | Bridgestone Corp | ゴム組成物 |
| DE19634971A1 (de) * | 1996-08-29 | 1998-03-05 | Wacker Chemie Gmbh | Flüssigsiliconkautschuk mit verbessertem Druckverformungsrest |
| WO2002010271A2 (en) * | 2000-07-31 | 2002-02-07 | Bridgestone Corporation | Properties of silica-filled rubber compounds with disulfane silica coupling agents at high mixing temperature |
| JP4622071B2 (ja) * | 2000-09-14 | 2011-02-02 | 東レ株式会社 | モノマー、ポリマー、眼用レンズおよびコンタクトレンズ |
| EP1394167B1 (de) * | 2001-08-06 | 2005-12-28 | Degussa AG | Organosiliciumverbindungen |
| DE10163941C1 (de) * | 2001-08-06 | 2003-04-10 | Degussa | Organosiliciumverbindungen, ein Verfahren zu ihrer Herstellung, sowie ihre Verwendung |
| DE50205449D1 (de) * | 2001-08-06 | 2006-02-02 | Degussa | Organosiliciumverbindungen |
| EP1298163B1 (de) * | 2001-09-26 | 2005-07-06 | Degussa AG | Geblockte Mercaptosilane, Verfahren zu deren Herstellung und die enthaltenden Kautschukmischungen |
-
2003
- 2003-06-20 DE DE10327624A patent/DE10327624B3/de not_active Expired - Fee Related
-
2004
- 2004-06-09 DE DE502004000168T patent/DE502004000168D1/de not_active Expired - Lifetime
- 2004-06-09 ES ES04013567T patent/ES2250943T3/es not_active Expired - Lifetime
- 2004-06-09 EP EP04013567A patent/EP1491547B1/de not_active Expired - Lifetime
- 2004-06-09 AT AT04013567T patent/ATE312108T1/de not_active IP Right Cessation
- 2004-06-09 PL PL04013567T patent/PL1491547T3/pl unknown
- 2004-06-16 MY MYPI20042329A patent/MY134485A/en unknown
- 2004-06-17 IL IL16262304A patent/IL162623A0/xx unknown
- 2004-06-17 TW TW093117553A patent/TWI353999B/zh not_active IP Right Cessation
- 2004-06-18 US US10/872,177 patent/US7423165B2/en active Active
- 2004-06-18 KR KR1020040045344A patent/KR101122952B1/ko active IP Right Grant
- 2004-06-18 MX MXPA04006052A patent/MXPA04006052A/es active IP Right Grant
- 2004-06-18 CN CNB2004100639685A patent/CN100390182C/zh not_active Expired - Fee Related
- 2004-06-18 JP JP2004181686A patent/JP4606785B2/ja not_active Expired - Fee Related
- 2004-06-18 UA UA20040604824A patent/UA81902C2/ru unknown
- 2004-06-21 BR BRPI0402414-1A patent/BRPI0402414B1/pt not_active IP Right Cessation
- 2004-06-21 RU RU2004118627/04A patent/RU2348642C2/ru not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| KR101122952B1 (ko) | 2012-03-15 |
| TWI353999B (en) | 2011-12-11 |
| BRPI0402414B1 (pt) | 2014-12-09 |
| DE502004000168D1 (de) | 2006-01-12 |
| ES2250943T3 (es) | 2006-04-16 |
| CN100390182C (zh) | 2008-05-28 |
| JP2005008639A (ja) | 2005-01-13 |
| CN1576279A (zh) | 2005-02-09 |
| RU2348642C2 (ru) | 2009-03-10 |
| IL162623A0 (en) | 2005-11-20 |
| JP4606785B2 (ja) | 2011-01-05 |
| BRPI0402414A (pt) | 2005-01-18 |
| KR20040111135A (ko) | 2004-12-31 |
| US20040266968A1 (en) | 2004-12-30 |
| DE10327624B3 (de) | 2004-12-30 |
| MXPA04006052A (es) | 2005-03-31 |
| TW200514815A (en) | 2005-05-01 |
| EP1491547A1 (de) | 2004-12-29 |
| RU2004118627A (ru) | 2006-01-10 |
| ATE312108T1 (de) | 2005-12-15 |
| EP1491547B1 (de) | 2005-12-07 |
| MY134485A (en) | 2007-12-31 |
| US7423165B2 (en) | 2008-09-09 |
| PL1491547T3 (pl) | 2006-04-28 |
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